A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17045577



Internal ID98147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32206095..32207608hg38UCSC Ensembl
chr11:32227641..32229154hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381514
hg191514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5499200
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17045577
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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